QC Chemist
1 month ago
To support new equipment qualification, lab computerized system and chemistry lab set up
To perform transfer/verification/validation of laboratory procedures within the team where required
To prepare technical documentation including but not limited to protocols, analytical write-ups, standard operating procedures, specifications, investigations and reports.
To perform analysis of incoming goods, intermediates and/or finished products under cGMP conditions for QC release or as part of stability studies.
To review analytical and laboratory data within the department for accuracy, completeness and compliance with detailed procedures.
To perform planned preventative maintenance and performance calibrations on equipment.
Management of QC chemical, reference standard and consumable stock levels
To maintain own training records and support and train other team members as required.
Participate/chip in Practical Process Improvement initiatives (PPI) or continuous improvement in the lab
Support and encourage a “Quality Culture” and company 4i values throughout QC
Ensure cGMP is applied in their area of work and align with cGMP in all areas of the business.
To work with HSE, cGMP and 5S in mind at all times.
Undertake ad-hoc activities that may be required by the business
To support shift work (if necessary) in future
Keys to Success:
Education
Degree in Chemistry or strongly related scientific field
Experience
At least 3 years relevant industrial experience
Ability to apply GMP regulations and other international guidelines to all aspects of the position.
Experience in equipment such as Capillary Electrophoresis (CE), Microplate Reader preferred
Ability to work independently and adhere to critical timelines
Excellent attention to detail
Excellent organisational skills
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